Canonical Allele Identifier: CA1763972859
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1802025903

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577882T>C , CM000670.2:g.11577882T>C GRCh38
NC_000008.10:g.11435391T>C , CM000670.1:g.11435391T>C GRCh37
NC_000008.9:g.11472800T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.784-488T>C